WO2007072116A1 - Appareil médical avec interface utilisateur améliorée - Google Patents

Appareil médical avec interface utilisateur améliorée Download PDF

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Publication number
WO2007072116A1
WO2007072116A1 PCT/IB2006/000203 IB2006000203W WO2007072116A1 WO 2007072116 A1 WO2007072116 A1 WO 2007072116A1 IB 2006000203 W IB2006000203 W IB 2006000203W WO 2007072116 A1 WO2007072116 A1 WO 2007072116A1
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WO
WIPO (PCT)
Prior art keywords
value
time
weight loss
profile
control system
Prior art date
Application number
PCT/IB2006/000203
Other languages
English (en)
Inventor
Fabio Roncadi
Marco Salsa
Matteo Malagoli
Glenn Sanders
Gary Warns
Original Assignee
Gambro Lundia Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=36870042&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2007072116(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Gambro Lundia Ab filed Critical Gambro Lundia Ab
Priority to CN2006800479645A priority Critical patent/CN101341489B/zh
Priority to ES06710311T priority patent/ES2388503T3/es
Priority to EP06710311A priority patent/EP1969507B1/fr
Priority to PL06710311T priority patent/PL1969507T3/pl
Publication of WO2007072116A1 publication Critical patent/WO2007072116A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
    • A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
    • A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
    • A61M1/1601—Control or regulation
    • A61M1/1613—Profiling or modelling of patient or predicted treatment evolution or outcome
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
    • G16H40/63—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/33—Controlling, regulating or measuring
    • A61M2205/3317—Electromagnetic, inductive or dielectric measuring means
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/33—Controlling, regulating or measuring
    • A61M2205/3324—PH measuring means
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/33—Controlling, regulating or measuring
    • A61M2205/3368—Temperature
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/50—General characteristics of the apparatus with microprocessors or computers
    • A61M2205/502—User interfaces, e.g. screens or keyboards
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/50—General characteristics of the apparatus with microprocessors or computers
    • A61M2205/502—User interfaces, e.g. screens or keyboards
    • A61M2205/505—Touch-screens; Virtual keyboard or keypads; Virtual buttons; Soft keys; Mouse touches
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/40—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mechanical, radiation or invasive therapies, e.g. surgery, laser therapy, dialysis or acupuncture
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S210/00—Liquid purification or separation
    • Y10S210/929—Hemoultrafiltrate volume measurement or control processes

Definitions

  • the invention relates to a medical apparatus with improved user interface.
  • the medical apparatus of the invention could be an apparatus intended for the extracorporeal treatment of blood, for instance by hemodialysis, hemofiltration, hemodialfitration, ultrafiltration, plasmapheresis or an apparatus for processing whole blood and/or blood components.
  • Blood treatment apparatus and similar medical devices comprise an extracorporeal circuit, provided with at least one blood treatment or blood processing unit, one tube, connecting a blood removal zone to said unit, and a second tube, extending downstream of the treatment or processing unit towards a blood return zone to the patient or towards a blood/blood components collection zone. Blood is moved from the patient or donor to the treatment or processing unit via pumps or other actuators controlled by the machine.
  • an adequately prepared dialysis liquid shall be sent to the treatment unit, and water removal through the treatment unit membrane as well other machine parameters shall be controlled.
  • a user can have the possibility to set a number of parameters in order to impose a specific prescription to a patient, such as for instance: flow rates of the various liquids, temperatures and conductivity of the liquids, concentration of the liquids used during treatment, flow rates of any anticoagulants used and delivered during treatment, pressures in the fluid conduits, net liquid removal rates of plasma water from whole blood and so on. It is therefore evident that users (the patient himself, a physician, a nurse) have normally a plurality of parameters to set before or even during the process performed by the medical apparatus.
  • Particularly important parameter are those that can take variable values or profiles through the treatment; referring to extracorporeal blood treatment these parameters can be ultrafiltration, conductivity of the dialysis liquid, concentration of a specific -substance in the dialysis liquid, flow rate of an infusion or substitution solution, temperature of the dialysis liquid, temperature of blood, temperature of an infusion solution, concentration of a certain specific drug that is delivered to the patient, etcetera.
  • the user interface is designed to allow easy and safe data entry.
  • a data entry user interface of general purpose and not specifically designed for the medical field is known from United States Patent 5,546,582.
  • This method comprises the following steps:
  • variable parameters i.e. parameters that can vary in the course of time during treatment.
  • US5247434 shows a method of programming a time-varying parameter comprising the steps:
  • This method allows the user to enter a profile curve and to move the ultrafiltration profile along the ordinates so as to achieve the desired integral value in the desired time frame.
  • a further user interface system for a dialysis machine is known from document US5788851.
  • This user interface does not specifically relate to data entry of profiles and comprises, in summary, the following features:
  • a touch screen displaying messages and information and permitting to select a parametric value pertinent to operation of said machine or pertinent to a treatment by said machine, - one hard key off of said touch screen, said touch screen prompting a user to press said hard key to signify that the selection of the parametric value has been completed;
  • control system having a host and a safety processing unit, wherein pressing of said hard key causes transfer of information relating to the selected parametric value from the host processing unit to the safety processing unit which is then checking said selected parametric value to confirm that said parametric value meets validation or safety criteria for a patient connected to said machine.
  • a further known technique is described in US6830693, which relates to a method of setting up a dialysis treatment in a dialysis machine comprising the steps of: determining conditions of a dialysis treatment adapted to a specific patient; determining a first function (U(t)) of a first quantity (U) characterizing the dialysis treatment as a function of time (t), the first function (U(t)) satisfying said conditions of the dialysis treatment and corresponding to a curve having a defined shape; and determining a second function (C(t)) of a second quantity (C) characterizing the dialysis treatment, the second function (C(t)) being correlated with the first function (U(t)) by constants (M, N) determined experimentally and the second function (C(t)) corresponding to a curve having a shape of the same kind as the shape of the first curve.
  • US reference US6881344 relates to a user interface and to a method of setting up a dialysis treatment in a dialysis machine wherein a group of parametric functions (U(t, P); C(t, P)) representing ultrafiltration or conductivity as a function of time (t) and of a parameter (P) are provided.
  • a group of parametric functions U(t, P); C(t, P) representing ultrafiltration or conductivity as a function of time (t) and of a parameter (P) are provided.
  • the present invention aims to further improve ease and reliability in data entry and visualization procedures for medical devices and particularly for blood treatment or blood processing machines wherein parameters variable in the course of a session need to be programmed.
  • the invention aims to reduce as possible the efforts for the user to configure, modify and execute settings relating to variable parameters. Moreover, the invention aims to render quick and intuitive creation and modification of profiles relating to variable parameters.
  • the invention aims to offer an efficient use of the memory resources of the system without impairing on usability.
  • the invention when for instance applied to the blood treatment area, the invention avoids to enter a reference profile that has to be stored, analyzed to determine which cumulative value (total weight loss if the profile is a weight loss rate profile) generates across a reference treatment time and then adapted to fit a desired cumulative value.
  • the profile of a certain parameter is calculated by the inventive solution to directly and immediately fit the desired cumulative value.
  • FIG. 1 is a schematic representation of a medical apparatus, for instance a blood treatment machine, according to the invention
  • FIG. 3 to 7 and 12 show a user interface according to the invention during the medical apparatus configuration
  • FIG. 8 shows a user interface according to the invention during the medical apparatus setup
  • FIG. 10 and 11 shows a flowchart of the working of an embodiment of a medical apparatus or user interface of the present invention.
  • reference number 1 denotes a medical apparatus.
  • the medical apparatus of the shown embodiment is a machine for the extracorporeal treatment of blood.
  • the medical apparatus of the invention could alternatively be a blood processing device or a blood component preparation device or other medical apparatus for fluid delivery/collection.
  • the apparatus shown in the enclosed drawings comprises a module 2 for preparing dialysis liquid to be sent into a first chamber 3 of a blood treatment unit 4, which is formed by a casing defining at least two chambers 3, 5 separated by a semipermeable membrane 6.
  • the dialysis preparation module 2 includes tubing 7 bringing dialysis liquid to the first chamber inlet, while a waste line 8 receives spent liquid exiting via an outlet of the first chamber.
  • the module 2 includes one or more concentrate containers 9, 10 delivering concentrated solutions, via respective lines 11 , 12 and upon the action of respective concentrate pumps 13, 14, into the tubing 7 thereby properly mixing water coming from a source 15 with said concentrates and obtaining the dialysis liquid.
  • Conductivity or concentration sensors 16, 17 can be provided on tubing 7 downstream each respective concentrate line. Said sensors provide control signals to a control system 18 which is responsible to then act on the concentrate pumps. Notice that sensors (not shown) detecting conductivity or concentration of electrolytes can also be present on the return tubing 8 containing waste liquid.
  • a pump 19 is generally operating on tubing 7 and a pump 20 on the waste line 8.
  • different alternative embodiments can be envisaged to bring dialysis liquid to the treatment unit with appropriate chemical and physical properties.
  • Fluid balance sensors for instance a first and a second flow-meter 21 , 22, operating on tubing 7 and on waste line 8 respectively, are used and are connected to the control system to provide signals necessary for regulating at least one of pumps 19, 20.
  • Other fluid balance systems can be used: scales for instance or balance chambers or any other volumetric or mass or flow-rate based system available to the skilled man.
  • an extracorporeal blood circuit is connected to the second chamber 5.
  • the extracorporeal circuit usually comprises at least an access branch 23 extending between a blood removal zone 24 from a patient or donor and the treatment unit 4, at least a return branch 25 extending downstream of the treatment unit, between the second chamber and a return zone of the blood to the patient; a peristaltic pump 26 is operatively associated to a length of pump tube of the extracorporeal circuit access branch.
  • a clamp or other closure device 27 can operate on the blood return branch 25, typically downstream from a gas separator 28.
  • access means are provided to the cardiovascular system of the patient, for example constituted by needles of appropriate sizes, catheters or accesses of different types.
  • One or more liquid infusion lines could be provided connected at one end to an infusion liquid source (a bag or in-line infusion liquid preparation system) and at the other end to the extracorporeal circuit, or directly to the patient or donor.
  • sensors such as pressure sensors 29, can be provided either on the extracorporeal circuit and/or on the dialysis liquid side of the apparatus.
  • sensors not herein disclosed in detail are provided with for directly or indirectly detecting the actual value of each machine or treatment parameter of interest, included those that can be set by the user, as it will appear from the following description.
  • the medical apparatus 1 above described represents a non-limiting example, which the present invention can be applied to.
  • the apparatus can of course include other components, which are not herein disclosed, as they are not relevant for the purpose of the understanding of present invention.
  • the apparatus 1 presents at least a user interface 30 for enabling setting of a plurality of parameters pertinent to operation of said apparatus or pertinent to a treatment to be performed by said apparatus.
  • the parameters pertinent to the apparatus operation can be settings for one or more actuators (pumps, warmers, valves, etcetera depending upon the apparatus), while the parameters relating to the treatment performed by the apparatus can be settings on prescription parameters that have to be achieved (in case of blood treatment these settings can be fluid removal rate, total weight loss in the course of a treatment session, achievement of a desired concentration of a substance(s) in blood, etcetera). It should be noted that some parameters can assume values variable in the course of the same treatment or procedure.
  • parameters which the operator could be interested to set can be the following: the rate of ultrafiltration in the course of a treatment (i.e. the amount of fluid per unit of time removed from blood through the membrane 6), the rate of infusion of a substance in the patient's or donor's blood, the conductivity or temperature or chemical concentration of a substance in a treatment liquid (for instance in the dialysis or in the infusion liquid), etcetera.
  • the present invention is mainly focused to how these kind of variable parameters (or profiles) are stored in the medical apparatus control system, as well as to how these profiles can be selected, modified, and actuated during a treatment session.
  • the user interface herein disclosed is connected with and part of the medical apparatus 1 , it shall be understood that the user interface 30 could be manufactured and sold separately and then connected to a medical apparatus.
  • the user interface 30 of the embodiment shown includes a screen 31, for instance a touch screen, which allows interaction with the user interface, for instance selection of certain parameters, visualization, either in analogical or in digital form, of values of said parameters arid display of other information as it will be here below in detail described. Please note that the enclosed figures ...
  • control system 18 which is connected to the user interface, is responsive to actions by a user on said user interface, and controls operations of the medical apparatus 1 by acting on a plurality of actuators (such as pumps 12, 13, 19, 20, 27, valve 27 and others) and by receiving signals by a plurality of sensors (such as for instance sensors 12, 13, 21, 22, 29 etc.).
  • actuators such as pumps 12, 13, 19, 20, 27, valve 27 and others
  • sensors such as for instance sensors 12, 13, 21, 22, 29 etc.
  • the control system of presently shown embodiment includes a main control unit, connected to the user interface 30, and at least a memory connected to the main control unit. From a technical point of view the main control unit includes at least a microprocessor, while the above-mentioned memory can be in a single physical memory or in physically separated memory devices.
  • control system 18 is programmed (for instance by loading a program in the memory which then is executed by the CPU) for defining on screen 31 an operating region 32, where a number of working displays can be displayed, and a navigation region 33, where a number of navigation keys can be displayed (see figure 2).
  • the working displays are shown one per time according to a sequence, which depends upon the sequence of activation of the navigation keys, as it will be apparent from below description.
  • the operating region 32 of the embodiment in figure 2 is adjacent to and in contact with the navigation region 33 and, in particular, is placed between the navigation region and a status bar region 34 extending transversally in the top part of the screen 31.
  • the navigation region of the non-limitative embodiments shown is in the bottom part of the screen and contains a plurality of navigation keys 35.
  • the control system displays in the working region a plurality of working displays 36, each including one or more indicia, such as touch buttons or touch icons 37, which can be selected to access particular submenus and/or for selecting a parameter or a group of parameters for successive modification of the value(s) thereof.
  • the medical apparatus could work according to different operating modes (for instance by way of non-limiting example idle mode, setup mode, priming mode, treatment mode, and rinse-back mode), the user interface reflects said operating modes in the status region 34.
  • each working display 36 can also display information, in alphanumeric or in analogical or in graphic form, regarding the status of the machine, its operating conditions, the current actual values of one or more parameters, etcetera.
  • each working display occupies the entire operating region, overlapping to or hiding previously displayed working displays.
  • the status bar in addition to information concerning the status mode of the machine (flushing, treatment, priming, rinse back, etc.) or can also provide alarm or information messages 34b (see figure 2).
  • the control system is programmed for associating each of said number of navigation keys 35 with a corresponding working display 36 so that each working display is selectable and displayable in the working region upon selection of the corresponding navigation key.
  • the user can therefore navigate through the various menus and sub-menus of the working display by acting on the navigation keys and on buttons appearing in the working display.
  • the above-disclosed non-limiting example of a navigation logic controlled by the control system allows the user to enter data and parameter values into the apparatus memory. Parameters having values, which should change in the course of the treatment or in the course of an operation (i.e. profiles), can also be entered via user interface 30.
  • Configuration is intended as the moment where the machine is neither running a treatment nor being submitted to preparation steps for running a treatment.
  • Configuration is normally executed when installing the machine or periodically by technically qualified people when updating the machine configuration.
  • the control system can be programmed to offer the operator to enter in configuration mode: access to configuration mode can be password protected as configuration should be a limited access environment for technically qualified personnel.
  • Shaping profiles are profiles, which are intended to represent the dynamic behavior taken by a first magnitude at the change of a second correlated magnitude. Shaping profile are not formed or defined by the actual values of a machine or patient parameters but are for instance non-dimensional or normalized representations of two correlated series of magnitudes.
  • Each shaping profile is stored in the control system memory as a plurality of pairs 39, 40, each pair including a reference value 39 and a respective time interval value 40.
  • Each time interval value can be a fraction of the total treatment time (for instance expressed as a percentage of the total treatment time) or a prefixed time interval (for instance expressed as a certain amount of seconds), while each reference value is stored as a fraction of total weight loss to be removed by a patient during total treatment time.
  • the embodiment of figure 3 shows a shaping profile 38 where percentages of a reference value 39 are correlated to corresponding percentages of time interval values 40.
  • the control system is programmed for storing up to a pre-fixed maximum number of time interval values for each shaping profile: in the enclosed embodiment the control system allows to enter up to 10 time interval values corresponding to 10 time intervals which could have or not the same duration.
  • Figure 4 shows the screen of figure 3 where a pop-up window 41 has been activated by the control system upon touch of the "edit selected profile" indicium 42 shown in figure 3.
  • Figure 4 shows in table form the ten steps of the shaping profile with the corresponding 10 time intervals values 40 (in percentages of total treatment time) and 10 reference values 39 (expressed in percentages of total weight loss).
  • control system can also be programmed for associating to each pair a third value 43 indicating whether the respective pair refers or not to a pure ultrafiltration treatment step wherein the spent liquid flowing in the waste line 8 is corporeal fluid only coming from the second chamber 3 of the treatment unit 4 via filtration through the semipermeable membrane of the filter unit.
  • control system could be programmed to store a plurality of shaping profiles.
  • the user interface screen displays a plurality of indicia 44 for allowing selection of the shaping profile: indeed the user can select and access a certain shaping profile for the purpose of simply visualizing it, or for modifying it or for creating a new profile.
  • the control system upon selection of the shaping profile, is programmed for displaying a graphic representation 45 of the selected shaping profile at least on a portion of said screen;
  • the graphic representation can be a Cartesian representation (a two axis plot as in figure 3) wherein reference values are represented as percentages of the total weight loss and time intervals as percentages of the total treatment time and/or a multi column table representation (see figure 4), wherein again reference values are represented as percentages of the total weight loss and time intervals as percentages of the total treatment time.
  • the resulting Cartesian representation is a histogram or bar graph wherein the height of each bar represents one of the values of each pair and wherein the thickness of each bar represents the other of the values in each pair.
  • the eight of each bar represents the percentage of weight loss and the thickness of each bar the percentage of treatment time during which said weight loss should be achieved.
  • the control system displays the mentioned editing indicium 42 on a portion of said screen: selection of the editing indicium moves the user into a new screen or screen area (in figure 4 the mentioned pop-up window 41) where the shaping profile reference values and corresponding time interval values of the selected profile are displayed and can be modified for creating a new shaping profile.
  • the operator can act on suitable means of the user interface to modify one or more steps of the shaping profile.
  • the control system of the enclosed embodiment is programmed for storing the new shaping profile if the sum of the reference values thereof and the sum of the time interval values do not exceed respective threshold values. For instance in case of values stored as percentages, the control system allows storage of a new profile or of a modified profile only if the sum of the values makes 100%.
  • the modification step comprises the following sub steps: displaying a graphic representation of said shaping profile (for instance in table form as in figure 4 or in Cartesian form), displaying at least a first indicium 45 allowing to select one of said plurality of pairs of the shaping profile, displaying a second indicium 46 allowing to modify the time interval value of the selected pair, displaying a third indicium 47 allowing to modify the reference value of the selected pair.
  • the first indicium can be a touch sensitive area comprising arrow keys 45a, 45b which when selected move a corresponding identifier 48 (which can be anything suitable for graphically or audibly identify a selection - in figure 4 the identifier is a background marking of the table line where the concerned pairs are represented) in correspondence of the selected step or pair to visually inform the user as to which values are under modification.
  • a corresponding identifier 48 which can be anything suitable for graphically or audibly identify a selection - in figure 4 the identifier is a background marking of the table line where the concerned pairs are represented
  • alternative means for identifying the pair under modification could be envisaged such as: directly touching the part of the screen where the pair is visually represented, or providing touch sensitive areas in correspondence of each representation of the pairs, etcetera.
  • the second indicium 46 and the third indicium 47 can be touch sensitive areas, such as buttons on the touch screen which, when selected, call on screen a respective data entry display 46a, 46b (such as a pad) for entering
  • each pair has a third value associated therewith
  • a fourth indicium 49 can be present for switching said third value between two conditions representing whether or not the respective pair is associated to a pure ultrafiltration step.
  • the fourth indicium can be an on/off switch or a touch sensitive area such as a button on the touch screen which, when selected, calls on screen a respective data entry display 49a (such as a pad - see the embodiment of figure) for allowing the user to specify "yes" (when UF only step is programmed) or "no" (if a non UF only step is programmed).
  • the left column indicates the operator's actions and the right column the apparatus reaction.
  • control system cold also be programmed so that, in configuration mode, a graphic representation 50 of the time varying parameter (in this case weight loss rate) is generated by the selected shaping profile 38 applying defaults values for total treatment time and total weight loss. This is made to give the operator programming a new shaping profile immediate feedback as to a corresponding behavior of the net weight loss rate with average values of total weight loss and total treatment time.
  • a graphic representation 50 of the time varying parameter in this case weight loss rate
  • the user interface enables setting of at least one time-varying parameter pertinent to operation of the apparatus or pertinent to a process to be performed by said apparatus.
  • the time-varying parameter is defined by a plurality of different parameter values that the parameter shall take during operation of the apparatus. The user can therefore set the time-varying parameter and program the machine to follow the parameter in the course of a determined time span.
  • control system In order to allow set up of the time-varying parameter, the control system is programmed for storing a plurality of shaping profiles, which form a shaping profiles library; the control system is programmed for allowing the user to select from the library of anyone of said shaping profiles. The control system then calculates the parameter values of the time-varying parameter starting from reference values of the selected shaping profile.
  • the control system stores a plurality of reference values defining the shaping profile, receives the value of at least a discriminating factor which relates to the time-varying parameter, and calculates each of the parameter values as a function of a corresponding reference value of the shaping profile and of the value of said discriminating factor.
  • the discriminating factor is a value that can be entered by the user (alternatively the control system could receive the value of the discriminating factor from other sources such as a patient card or a remote unit) and can represent one of the following values, which characterize the time-varying parameter:
  • the reference values of the shaping profiles are expressed as percentages of the discriminating factor value and calculation of each parameter value comprises the step of multiplying each reference value by the value of said discriminating factor.
  • the shaping profile is stored as a plurality of pairs, each pair including a shaping profile reference value and a time interval value.
  • Each time interval value is either a fraction (for instance expressed as a percentage of total treatment time) of the total treatment time or a prefixed time interval.
  • the control system is programmed to receive said discriminating factor value and a total treatment time value (or several prefixed time interval values), and to calculate a profile for said time-varying parameter as function of the values of said plurality of pairs, of said discriminating factor value and, if time fractions are used, of the treatment time. More in detail the calculation comprises determining each of said plurality of parameter values by multiplying each reference value by the value of the discriminating factor divided by the time interval value, or the value of the discriminating factor, or a value proportional to the value of the discriminating factor. Then each parameter value is associated with the respective actual time interval during which the parameter value remains constant for forming a step shaped profile of said time-varying parameter.
  • control system can be programmed to check the sum of the reference values and to generate an error signal if the sum is higher than a reference threshold value, and/or to check the sum of the time interval values and to generate an error signal if the sum is higher than a reference threshold value.
  • the time-varying parameter can be any parameter that the user may want to set at values varying in the course of the dialysis treatment session.
  • a time varying parameter could be one of the following:
  • the time-varying parameter is the net weight loss rate (which in pure hemodialysis with no infusion corresponds to the ultrafiltration rate) and the discriminating factor value is the total weight loss to be achieved at the end of the total treatment time.
  • the control system is then programmed to receive the value of the total weight loss as discriminating factor and a total treatment time, and to calculate a profile for said time-varying parameter as function of said plurality of reference value of the shaping profile, of said discriminating factor value and of the treatment time.
  • the shaping profile can be stored as a plurality of pairs where each pair includes a shaping profile reference value and a time interval value representing the time span during which the reference value applies.
  • the reference values are represented as fraction of the total weight loss, while each time interval value is represented either as fraction of the total treatment time or as a prefixed actual time interval.
  • the shaping profile reference values can be stored as percentages of the total weight loss and the time interval values of the shaping profile as percentages of the total treatment time.
  • the time varying profile would be calculated starting from the shaping profiles pairs and multiplying each reference value of the pair times the total weight loss value and multiplying each time interval value times the total treatment time thereby obtaining a plurality of pair defining the time varying profile.
  • control system can be programmed for storing a plurality of shaping profiles to form a shaping profiles library; referring to figure 8 embodiment where the blood treatment apparatus user interface has a touch screen, each shaping profile can be selected by a corresponding touch sensitive indicium 51 , which is basically analogous to indicia 44 but for the fact that the machine is in setup mode.
  • control system allows selection of the total weight loss and of the total treatment time by means a data entry unit. The operator would then be allowed to select from the library anyone of, the shaping profiles.
  • the control system determines the plurality of pairs representing the profile of the time-varying parameter (each pair including a weight loss rate value and the corresponding actual time interval value during which the weight loss rate is constant) multiplying the time interval values by the total treatment time value to obtain actual time intervals and multiplying the shaping profile reference values by the value of the total weight loss divided by the respective actual time interval.
  • the control system can display the time-varying weight loss rate profile 52 on an area 53 of the screen.
  • the discriminating value can for instance be equal to 10kg (overall weight loss)
  • the total treatment time can be set at 3 hours and the selected shaping profile could be characterized by 3 the reference values having the following values 10%, 40%, 50% (expressed as percentages of the total weight loss) and 3 corresponding time intervals of 1 hour each (which could alternatively be expressed in percentage term as 33%, 33%, and 33%).
  • Each value of the time varying profile (weight loss rate profile) would be calculated multiplying each percentage value times the value of the discriminating value thus obtaining 1kg, 4kg, and 5kg and then dividing each of these values by the respective time interval of relevance.
  • the time varying profile would then be characterized by a first step of 1kh/hour for the first hour, by a second step of 4kg/hour for the second hour and by a third step of 5kg/hour for the third hour.
  • the control system can be programmed for allowing selection from the library of anyone of the stored shaping profiles and allowing selection of the total weight loss.
  • each pair of the time varying parameter actual profile (defined as a weight loss rate value and corresponding prefixed actual time interval value during which the weight loss rate is constant) would be calculated multiplying the shaping profile reference values by the value of the total weight loss and divided by the respective prefixed actual time interval.
  • the machine control system is programmed so that during setup mode of the machine the operator has to first select or render available to the control system the total weight loss and the total treatment time before being allowed to access selection of the desired shaping profile.
  • the total weight loss and/or the total treatment time are not available to the control system said touch sensitive indicia are either switched to a condition where they are disabled and not touch sensitive or they are simply not displayed at all.
  • the reference profiles values could be stored as percentages of said average weight loss rate and the time intervals stored as prefixed values: in this case the machine calculates the profile by multiplying each reference value times the weight loss rate (this giving a profile of weight loss rates applicable during a prefixed treatment time); while running the treatment, the control system cyclically and continuously applies the profile as many time as necessary.
  • control system allows the user to modify the actual profile of the time-varying parameter.
  • the modification of the profile is similar to the modification of the shaping profiles in configuration mode: notice however that modification of the actual profile in setup mode differs from modification of the shaping profiles during machine configuration, in that the profiles here are not described in terms of percentages, but in terms of their actual values calculated using the entered weight loss and treatment time total values.
  • control system allows storing the new shaping profile if the sum of the reference values thereof and the sum of the time interval values do not exceed the total treatment time and the total weight loss.
  • the modification of the profile comprises displaying a graphic representation 56 of said profile (in table and/or in plot form) and displaying the following indicia (which in case of a touch screen are touch sensitive areas or buttons): a first indicium 57 allowing to select one of said plurality of pairs of the shaping profile, a second indicium 58 allowing to modify the time interval value of the selected pair, a third indicium 59 allowing to modify the reference value of the selected pair, and a fourth indicium 60 for switching said third value between two conditions representing whether or not the respective pair is associated to a pure ultrafiltration step.
  • the selection of said indicia can call a respective pop-up window allowing the user to enter the new desired values as in configuration mode for the shaping profiles.
  • control system could also be programmed for allowing entry of a plurality of reference values and corresponding time interval values of the new profile.
  • new profile can be stored in the profiles library only after verifying if the sum of the reference values and the sum of the time interval values do not exceed respective threshold values and transformed, before storage, into normalized values by dividing the absolute values of weight loss rate and time interval by total treatment time and total weight loss to generate a shaping profile.
  • the user is can activate the dialysis treatment.
  • the apparatus runs the treatment at a constant weight loss rate, which can be either a default value or a value set by the operator. Even when the treatment starts at constant weight loss rate, still the control system can be programmed for allowing selecting a shaping profile after treatment start, computing the profile of the net weight loss rate using:
  • the control system can also be programmed for allowing modification of the total treatment time and/or total weight loss while treatment is in progress.
  • the control system recalculates the weight loss rate profile data using the selected shaping profile and the new treatment time, taking into account the amount of time that has already since treatment start.
  • the control system is programmed for recalculating the weight loss rate profile data using the selected shaping profile and the new weight loss, taking into account the amount of fluid that has already been removed since treatment start.
  • control system is programmed for setting the net weight loss rate to a constant value equal to the difference (target total weight loss - already removed fluid) divided by the time remaining in the treatment.
  • a further separate feature of the invention consists in that the control system is programmed for starting an error compensation procedure if the set total weight loss cannot be reached using the set weight loss rate profile; the compensation procedure is useful for instance when the machine has not achieved in reality the weight loss the operator expected with the set profile (this could happen in case of malfunctioning for instance).
  • the compensation procedure is also useful if the user modifies in the course of the treatment the desired weight loss and/or treatment time in a way that the set profile is unable to fulfill.
  • the compensation procedure which can be started by the operator or automatically started by the control system, comprises the following steps:
  • the control system is programmed for comparing each value of the weight loss rate profile with an acceptable threshold checking if all steps of the of the weight loss rate profile are greater than or equal to the minimum allowed UF value and if all steps of the ultrafiltration profile are lower than a maximum allowed UF value.
  • the control system during setup, or during dialysis, or during compensation allows storing and execution of a profile only if above check is positively passed.
  • a possible embodiment and working of the present invention during set-up is described here below with the aid of the flowchart shown in figures 10 and 11.
  • the user inserts Dialysis Total treatment Time (T) and Total Weight Loss (TWL).
  • the user by operating on navigation keys 35 can access screen of figure 12 and enter TWL and T using touch buttons 61 and 62.
  • the control system cannot create an actual weight loss rate profile without the selected shaping profile and the values of TWL and T.
  • the user must insert T and TWL in order to make available the Choose Profile Button 63 which is showing two selectable types of parameters: sodium or UF (weight loss rate).
  • the user presses button 63 and enters the screen of figure 8 where he has then to select the desired Profile (step 101 in the flowchart of figures 10 and 11) and the control system can then calculate a real Profile, using the percentages of the shaping profile, T and TWL (step 102).
  • the weight loss rate (UFR) represented by the actual weight loss rate profile must, at each time step, be greater-equal than a minimum (MinUFR) and less-equal than a maximum (MaxUFR).
  • the control system therefore starts a routine (step 104 in figure 10) that checks if there are points on the profile out of the range [MinUFR, MaxUFR]. If all the profile is inside this interval, the control system displays it and the user can confirm it (steps 105 an 106 in figure 11).
  • the routine finds points out of range, it clips the points (step 107 in figure 11): this means that a value less then MinUFR is set to MinUFR and a value greater than MaxUFR is set to MaxUFR (refer for instance to figure 9 where weight loss rates higher than 4kg/h are set at 4kg/h).
  • the left column indicates the operator's actions and the right column the apparatus reaction.
  • the invention also concerns a software program comprising instructions which, when executed by the main control system of the apparatus 1 or of the user interface, programs the control system to execute the control system steps which have been already disclosed in the chapter 'user interface' and therefore not herein repeated.
  • the software program can be stored in any adequate support and then sold separately from the medical apparatus 1.
  • the software program could be stored on a magnetic recording support (for instance an hard disk, a cassette, a floppy disk, etcetera), or on an optical recording support (DVD or CD or other), on an electrical or electromagnetic carrier signal (if for instance the program is sent via a network), or on a computer readable memory (ROM, EPROM, RAM), or other convenient support memory device and then associated to the apparatus control system which running the program stored on said support is then programmed to render available a user interface having the features above described.

Abstract

L’appareil médical (1) de l’invention comprend un système de commande permettant le stockage de plusieurs profils de mise en forme. Chaque profil de mise en forme (38) est stocké en tant que multiples paires (39, 40) incluant une valeur de référence de profil de mise en forme et une valeur d’intervalle de temps. La valeur de référence est représentée en tant que fraction, par exemple un pourcentage, de la perte totale de poids que l’appareil doit obtenir à la fin d’une durée de traitement. Chaque valeur d’intervalle de temps est représentée soit en tant que fraction de la durée totale de traitement, soit en tant qu’intervalle de temps réel préfixé. Le système de commande calcule le taux de perte de poids réel par rapport au profil de temps en fonction de la perte de poids totale désirée, de la durée totale de traitement désirée ainsi que d’un profil de mise en forme désiré sélectionné.
PCT/IB2006/000203 2005-12-19 2006-02-03 Appareil médical avec interface utilisateur améliorée WO2007072116A1 (fr)

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CN2006800479645A CN101341489B (zh) 2005-12-19 2006-02-03 具有改进用户界面的医疗设备
ES06710311T ES2388503T3 (es) 2005-12-19 2006-02-03 Aparato médico con interfaz de usuario mejorada
EP06710311A EP1969507B1 (fr) 2005-12-19 2006-02-03 Appareil médical avec interface utilisateur améliorée
PL06710311T PL1969507T3 (pl) 2005-12-19 2006-02-03 Aparat medyczny z ulepszonym interfejsem użytkownika

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US20030018395A1 (en) * 2001-07-18 2003-01-23 Crnkovich Martin J. Method and system for controlling a medical device

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2436405A1 (fr) * 2010-09-29 2012-04-04 Terumo Kabushiki Kaisha Appareil médical domestique
US9069886B2 (en) 2010-09-29 2015-06-30 Terumo Kabushiki Kaisha Home medical apparatus
US10391218B2 (en) 2012-09-28 2019-08-27 Gambro Lundia Ab Extracorporeal blood treatment apparatus and method of setting an extracorporeal blood treatment
US11007309B2 (en) 2012-09-28 2021-05-18 Gambro Lundia Ab Extracorporeal blood treatment apparatus and method of setting an extracorporeal blood treatment

Also Published As

Publication number Publication date
PL1969507T3 (pl) 2012-09-28
CN101341489A (zh) 2009-01-07
US20110284464A1 (en) 2011-11-24
US7988850B2 (en) 2011-08-02
EP1969507A1 (fr) 2008-09-17
CN101341489B (zh) 2012-10-03
EP1969507B1 (fr) 2012-05-16
US8287736B2 (en) 2012-10-16
ES2388503T3 (es) 2012-10-16
US20070138069A1 (en) 2007-06-21

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